Carbon-13 Nuclear Magnetic Resonance Spectroscopy: Carbon-13 Chemical Shifts and Coupling Constants

作者: E.F. Mooney , P.H. Winson

DOI: 10.1016/S0066-4103(08)60322-1

关键词: Carbon-13 NMRCarbon-13PolarNuclear magnetic resonance spectroscopyChemistryChemical shiftChemical physicsAnalytical chemistryCoupling constantCoupling (physics)Resonance

摘要: Publisher Summary This chapter deals with the chemical-shift correlations within different classes of organic compounds and also focuses on 13 C coupling constants. The developments in instrumentation measurement techniques that may be utilized for NMR are discussed chapter. In order to overcome low natural abundance sensitivity isotope, large sample tubes high values r.f. power have generally been used observe resonance signals. Flow avoid difficulties from saturation improved can achieved, by using internuclear double technique (INDOR). Enhancement signals obtained, examining presence free radicals. Proton-decoupling techniques, addition increasing signal intensity collapse C– 1 H coupling, give rise overhauser enhancement. Later, theoretical considerations provided carbon-13 chemical shifts nuclear spin-spin involving carbon-13. simple unsubstituted hydrocarbons predicted, additivity relations, although there serious deviations constitutive rule when substituted polar groupings. alicyclic provides information regarding conformational preference rings.

参考文章(189)
William B. Smith, Ben A. Shoulders, The nuclear magnetic resonance spectra of some 9,10-bridged 9,10-dihydroanthracenes The Journal of Physical Chemistry. ,vol. 69, pp. 2022- 2026 ,(1965) , 10.1021/J100890A037
George B. Savitsky, Keishi Namikawa, Carbon-13 Chemical Shift Viewed as a Constitutive Property. I. Unsubstituted Hydrocarbons The Journal of Physical Chemistry. ,vol. 68, pp. 1425- 1428 ,(1964) , 10.1021/J100789A047
E. Alexander. Hill, John D. Roberts, A Reinterpretation of the Nuclear Magnetic Resonance Spectrum of Cyclobutene Journal of the American Chemical Society. ,vol. 89, pp. 2047- 2049 ,(1967) , 10.1021/JA00985A013
A. Mathias, Carbonyl C13 chemical shifts in substituted benzaldehydes Tetrahedron. ,vol. 22, pp. 217- 223 ,(1966) , 10.1016/0040-4020(66)80121-7
Theodore Vladimiroff, Edmund R. Malinowski, Substituent Effects. VI. Theoretical Interpretation of Additivity Rules of NMR Using McWeeny Group Functions The Journal of Chemical Physics. ,vol. 46, pp. 1830- 1841 ,(1967) , 10.1063/1.1840942
K. S. Dhami, J. B. Stothers, 13C N.M.R. STUDIES: PART V. CARBON-13 SPECTRA OF SOME SUBSTITUTED STYRENES Canadian Journal of Chemistry. ,vol. 43, pp. 510- 520 ,(1965) , 10.1139/V65-066
H. L. Retcofsky, Robert A. Friedel, Carbon-13 nuclear magnetic resonance studies of 4-substituted pyridines The Journal of Physical Chemistry. ,vol. 71, pp. 3592- 3596 ,(1967) , 10.1021/J100870A038
Isadore B. Berlman, Hermann O. Wirth, O. J. Steingraber, Anomalous fluorescence characteristics of fluoranthene and some of its derivatives Journal of the American Chemical Society. ,vol. 90, pp. 566- 569 ,(1968) , 10.1021/JA01005A003
Kensuke Takahashi, Tyo Sone, Yasuo Matsuki, Genjiro Hazato, PMR Studies of Bromothiophenes Bulletin of the Chemical Society of Japan. ,vol. 38, pp. 1041- 1043 ,(1965) , 10.1246/BCSJ.38.1041